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1992 - 2002年澳大利亚和新西兰晚发型新生儿革兰氏阴性杆菌感染情况

Late onset neonatal Gram-negative bacillary infection in Australia and New Zealand: 1992-2002.

作者信息

Gordon Adrienne, Isaacs David

机构信息

Department of Neonatal Medicine, Royal Prince Alfred Hospital, Sydney, Australia.

出版信息

Pediatr Infect Dis J. 2006 Jan;25(1):25-9. doi: 10.1097/01.inf.0000195628.35980.2e.

Abstract

BACKGROUND

Late onset neonatal Gram-negative bacillary infection is a significant cause of morbidity and mortality.

OBJECTIVE

To determine the incidence and mortality from late onset Gram-negative bacillary infections in neonatal units.

METHODS

An 11-year longitudinal prospective surveillance study. Clinicians in 20 neonatal units in Australia and New Zealand collected data. Late onset sepsis was defined as clinical signs of infection starting more than 48 hours after birth, with laboratory evidence supporting sepsis and pure growth of a pathogen from blood and/or cerebrospinal fluid.

RESULTS

Overall, 702 of 3113 (22.5%) episodes of late onset sepsis in 681 infants were from Gram-negative bacilli. Overall mortality was 20.8% (142 of 681 infants) and significantly related to maturity, birth weight and infecting organism. Mortality was 25% for infants <30 weeks compared with 11.5% for infants > or =30 weeks gestation (P < 0.0001) and 24.2% for infants with birth weights <1500 g versus 12.7% if > or =1500 g (P < 0.0001). Infection by Pseudomonas aeruginosa was associated with 52.3% mortality (46 of 88 infants), significantly higher than the 13.7% to 23.8% fatality from other Gram-negative bacilli (P < 0.0001). During the surveillance, the late onset Gram-negative bacillary infection rate remained stable at 1.14 per 1000 live births (range 0.87-1.5). Similarly, mortality was unchanged, being 0.25 per 1000 live births (range 0.12-0.43).

CONCLUSIONS

Gram-negative bacilli remain important causes of late onset neonatal sepsis, especially among very low birth weight infants, and result in a high mortality, particularly with P. aeruginosa infections.

摘要

背景

晚发性新生儿革兰氏阴性杆菌感染是发病和死亡的重要原因。

目的

确定新生儿病房晚发性革兰氏阴性杆菌感染的发病率和死亡率。

方法

一项为期11年的纵向前瞻性监测研究。澳大利亚和新西兰20个新生儿病房的临床医生收集数据。晚发性败血症定义为出生后48小时以上出现感染的临床体征,并有实验室证据支持败血症,且血液和/或脑脊液中病原菌纯培养生长。

结果

总体而言,681例婴儿的3113次晚发性败血症发作中,702次(22.5%)由革兰氏阴性杆菌引起。总体死亡率为20.8%(681例婴儿中的142例),且与成熟度、出生体重和感染病原体显著相关。孕周<30周的婴儿死亡率为25%,而孕周≥30周的婴儿死亡率为11.5%(P<0.0001);出生体重<1500g的婴儿死亡率为24.2%,而出生体重≥1500g的婴儿死亡率为12.7%(P<0.0001)。铜绿假单胞菌感染的死亡率为52.3%(88例婴儿中的46例),显著高于其他革兰氏阴性杆菌的13.7%至23.8%的死亡率(P<0.0001)。在监测期间,晚发性革兰氏阴性杆菌感染率保持稳定,为每1000例活产1.14例(范围0.87 - 1.5)。同样,死亡率没有变化,为每1000例活产0.25例(范围0.12 - 0.43)。

结论

革兰氏阴性杆菌仍然是晚发性新生儿败血症的重要原因,尤其是在极低出生体重儿中,并且导致高死亡率,特别是铜绿假单胞菌感染。

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